1. Experienced in independent instrumental analysis of raw material, in process samples, finished product and stability samples of pharmaceutical products. 2. Well versed in analysis of Tablets, capsules, liquids samples, for common test as Assay, Related substances, Dissolution and preservative content analysis as per controlled specification and method of analysis. 3. Should able to operate, calibrate and maintain instruments like HPLC, GC, Dissolution apparatus, UV and FTIR etc. 4. Experience of Empower, Lab solution software shall be recommended. 5. Aware about on line & good documentation practices. 6. Should strictly adhere to SOPs and specification. 7. Should have knowledge of Data integrity and QMS. 8. Should able to maintain cGMP, safety throughout the activities done in the laboratory. 9. Microsoft word, excel & ppt experience is must. 10. Exposure to perform AMV or development shall be preferred. 11. Candidate having knowledge of ICH guideline is preferred.
M.Sc Chemistry
